Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Fam221a ENSRNOG00000009447

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Description

family with sequence similarity 221, member A [Source:RGD Symbol;Acc:1563175]

Gene Synonyms

LOC500118, MGC114484

Location

Primary_assembly 4: 79,667,284-79,689,761 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 4 transcripts (splice variants), 182 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000012677.9	Fam221a-201	1684	351aa	ENSRNOP00000012677.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q627	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSRNOT00000067125.4	Fam221a-202	1456	249aa	ENSRNOP00000060562.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JSY5	-
ENSRNOT00000097852.2	Fam221a-203	1016	301aa	ENSRNOP00000081618.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G875	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSRNOT00000098105.2	Fam221a-204	887	258aa	ENSRNOP00000084912.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A066	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,

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Summary

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